Gen-Panel
Weibliche Infertilität, umfassende Diagnostik: ID389.00, 80 Gene
ASTL,
BMP15,
BNC1,
BTG4,
C14orf39,
CDC20,
CHEK1,
CLPP,
CYP11A1,
CYP11B1,
CYP17A1,
CYP21A2,
DAP3,
DIAPH2,
ERAL1,
ERCC6,
ESR2,
FANCM,
FBXO43,
FIGLA,
FMR1,
FOXL2,
FSHR,
GDF9,
HARS2,
HFM1,
HROB,
HSD3B2,
HSD17B4,
HSF2BP,
INHA,
KASH5,
KHDC3L,
KPNA7,
LARS2,
LHCGR,
MCM8,
MCM9,
MEI1,
MEIOB,
MGA,
MOS,
MRPS22,
MSH4,
MSH5,
NHEJ1,
NLRP2,
NLRP5,
NLRP7,
NOBOX,
NR5A1,
NUP107,
PABPC1L,
PADI6,
PANX1,
PATL2,
POF1B,
POR,
PSMC3IP,
REC114,
SOHLH1,
SPATA22,
SPIDR,
STAG3,
STAR,
SYCE1,
SYCP2L,
TLE6,
TOP6BL,
TP63,
TRIP13,
TUBB8,
TWNK,
WEE2,
XRCC2,
ZFP36L2,
ZP1,
ZP2,
ZP3,
ZSWIM7
HPO Terms
Primary amenorrhea, Secondary amenorrhea, Premature ovarian insufficiency, Hypergonadotropic hypogonadism, Increased serum FSH level, Increased serum LH level, Decreased serum estradiol level, Decreased antral follicle count, Ovarian dysgenesis, Ovarian failure, Ovarian hypoplasia, Aplasia/hypoplasia of the ovaries, Abnormality of menstrual cycle, Hypoplastic uterus, Müllerian agenesis, Uterine aplasia, Congenital uterine malformation, Ovarian cyst, Decreased ovarian reserve, Ovarian agenesis
